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Comparison · NCT05732454-85b67d24

DB Period: Etrasimod 2 mg vs DB Period: Placebo: Part 1, DB Period: Number of Participants With Laboratory Test Abnormalities

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. DB Period: Etrasimod 2 mg vs DB Period: Placebo: Part 1, DB Period: Number of Participants With Laboratory Test Abnormalities. Trial comparisons, record NCT05732454-85b67d24. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05732454-85b67d24

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.7590.5790.878wilson
Risk in group 20.4810.3070.66wilson
Risk difference, group 1 minus group 20.2770.02370.488newcombe hybrid score
Risk ratio, group 1 over group 21.581.012.45log
Odds ratio, group 1 over group 23.381.0910.6log
Number needed to treat, for one more participant with the outcome on DB Period: Etrasimod 2 mg than on DB Period: Placebo3.612.0542.1from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1DB Period: Etrasimod 2 mgParticipants who received etrasimod 2 mg orally once daily for 16 weeks in DB period of Part 1.2229OG000
Group 2DB Period: PlaceboParticipants who received placebo matched to etrasimod orally once daily for 16 weeks in DB period of Part 1.1327OG001

Outcome

Type
PRIMARY
Title
Part 1, DB Period: Number of Participants With Laboratory Test Abnormalities
Description
Laboratory assessments included hematology, clinical chemistry, urinalysis, other parameters and reflex tests. Number of participants with abnormalities in any of laboratory parameters is reported.
Time frame
DB Period: From first dose of study drug up to 16 Weeks of treatment
Population
DB period: Safety analysis set included of all participants who were randomized and received at least 1 dose of study drug in DB period. Here, Overall Number of Participants Analyzed signifies number of participants evaluable for this outcome measure.

Source ClinicalTrials.gov

Trial

Title
A Study to Learn About the Study Medicine Etrasimod in Adults With Moderate to Severe Atopic Dermatitis (AD) Who Have Already Tried Treatments Taken by Mouth or by Injection
NCT number
NCT05732454
Phases
PHASE2, PHASE3
Conditions
Atopic Dermatitis, Atopic Dermatitis, Unspecified, Eczema, Eczema, Atopic
Interventions
etrasimod, Placebo
Lead sponsor
Pfizer
Results first posted
2025-05-08

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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